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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

methyl 2-(2,5-dimethyl-1,3-thiazol-4-yl)acetate

COC(=O)Cc1nc(sc1C)C Request for Quotation
Chemical Name: methyl 2-(2,5-dimethyl-1,3-thiazol-4-yl)acetate
CAS Number: 306937-37-1
Product Number: AG0030YZ(AGN-PC-0KLBV7)
Synonyms:
MDL No:
Molecular Formula: C8H11NO2S
Molecular Weight: 185.2434

Identification/Properties

Properties
BP:
263.7°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Computed Properties
Molecular Weight:
185.241g/mol
XLogP3:
1.6
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
3
Exact Mass:
185.051g/mol
Monoisotopic Mass:
185.051g/mol
Topological Polar Surface Area:
67.4A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
174
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


Methyl 2-(2,5-dimethylthiazol-4-yl)acetate plays a crucial role in chemical synthesis as a versatile building block. Its unique structure enables it to participate in various reactions, such as esterification, acylation, and nucleophilic substitution. This compound serves as an important intermediate for the synthesis of pharmaceuticals, agrochemicals, and fine chemicals due to its reactivity and compatibility with a wide range of functional groups. Its presence in the synthesis route facilitates the introduction of the thiazole moiety into the target molecule, imparting desired biological or chemical properties. Additionally, the methyl ester group enhances the compound's solubility and stability, making it an ideal candidate for complex synthetic pathways.